ENST00000369409.9:c.458T=
|
ENSP00000358417.5:p.Leu153=
|
|
ENST00000462324.2:n.541T=
|
|
|
ENST00000641023.2:c.458T=
MANE Select
|
ENSP00000493175.1:p.Leu153=
|
|
ENST00000641074.1:c.458T=
|
ENSP00000493446.1:p.Leu153=
|
|
ENST00000641115.1:c.458T=
|
ENSP00000493264.1:p.Leu153=
|
|
ENST00000641213.1:c.*111T=
|
ENSP00000493079.1:n.*111T=
|
|
ENST00000641247.1:c.*177T=
|
ENSP00000492955.1:n.*177T=
|
|
ENST00000641272.1:c.392T=
|
ENSP00000493432.1:p.Leu131=
|
|
ENST00000641314.1:n.443T=
|
|
|
ENST00000641371.1:c.372T=
|
ENSP00000493305.1:p.Pro124=
|
|
ENST00000641375.1:c.*294T=
|
ENSP00000493089.1:n.*294T=
|
|
ENST00000641455.1:n.3T=
|
|
|
ENST00000641491.1:c.*111T=
|
ENSP00000493187.1:n.*111T=
|
|
ENST00000641570.1:c.*177T=
|
ENSP00000493213.1:n.*177T=
|
|
ENST00000641573.1:n.546T=
|
|
|
ENST00000641587.1:c.*169T=
|
ENSP00000493453.1:n.*169T=
|
|
ENST00000641597.1:c.458T=
|
ENSP00000493382.1:p.Leu153=
|
|
ENST00000641711.1:n.682T=
|
|
|
ENST00000641756.1:c.*202T=
|
ENSP00000493147.1:n.*202T=
|
|
ENST00000641811.1:c.214T=
|
|
|
ENST00000641847.1:n.317T=
|
|
|
ENST00000641891.1:c.*284T=
|
ENSP00000493288.1:n.*284T=
|
|
ENST00000641927.1:n.398T=
|
|
|
ENST00000641947.1:c.458T=
|
ENSP00000492994.1:p.Leu153=
|
|
ENST00000642021.1:n.580T=
|
|
|
ENST00000642041.1:c.*497T=
|
ENSP00000493415.1:n.*497T=
|
|
ENST00000369407.3:c.356T=
|
ENSP00000358415.3:p.Leu119=
|
|
ENST00000369409.8:c.458T=
|
ENSP00000358417.4:p.Leu153=
|
|
ENST00000462324.1:n.726T=
|
|
|
ENST00000493622.5:n.647T=
|
|
|
NM_006623.3:c.458T=
|
NP_006614.2:p.Leu153=
|
|
XM_011541226.1:c.680T=
|
XP_011539528.1:p.Leu227=
|
|
XM_011541227.1:c.602T=
|
XP_011539529.1:p.Leu201=
|
|
XM_011541228.1:c.569T=
|
XP_011539530.1:p.Leu190=
|
|
XM_011541229.1:c.395T=
|
XP_011539531.1:p.Leu132=
|
|
XM_011541230.1:c.173T=
|
XP_011539532.1:p.Leu58=
|
|
XM_011541231.1:c.164T=
|
XP_011539533.1:p.Leu55=
|
|
XM_011541226.2:c.680T=
|
XP_011539528.1:p.Leu227=
|
|
XM_011541227.2:c.602T=
|
XP_011539529.1:p.Leu201=
|
|
XM_011541228.2:c.569T=
|
XP_011539530.1:p.Leu190=
|
|
XM_011541231.2:c.164T=
|
XP_011539533.1:p.Leu55=
|
|
XM_024446338.1:c.569T=
|
XP_024302106.1:p.Leu190=
|
|
NM_006623.4:c.458T=
MANE Select
|
NP_006614.2:p.Leu153=
|
|